rs36211723, MYBPC3

N. diseases: 5
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Familial Hypertrophic Cardiomyopathy Type 4
CUI: C1861862
Disease: Familial Hypertrophic Cardiomyopathy Type 4
145 0.851 0.080 11 47338520 missense variant C/G;T snv 1.6E-05 0.800 1.000 26 1995 2017
Cardiomyopathy, Hypertrophic, Familial
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
355 0.851 0.080 11 47338520 missense variant C/G;T snv 1.6E-05 0.700 1.000 8 2004 2015
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.851 0.080 11 47338520 missense variant C/G;T snv 1.6E-05 0.700 1.000 7 2004 2017
Conduction disorder of the heart
CUI: C0264886
Disease: Conduction disorder of the heart
11 0.851 0.080 11 47338520 missense variant C/G;T snv 1.6E-05 0.700 0
LEFT VENTRICULAR NONCOMPACTION 10
CUI: C3715165
Disease: LEFT VENTRICULAR NONCOMPACTION 10
20 0.851 0.080 11 47338520 missense variant C/G;T snv 1.6E-05 0.700 0